vialroom

#coa-reading 2026-05-13

Wednesday56 messages12 participantstimes are UTC
Highlights from this day
  • assay_not_purity — a lab that reports "greater than 98%" rather than a number is telling you they did not integrate carefully, thats just me 09:23
  • olive_orders — the related substances table is the interesting part. a row of "not detected" means they did not look hard, ill dig out the number 10:09
  • deamidation — update from 16 months ago: started asking every supplier for water content and about half now include it 10:17
  • typosquat_tay — sorry to jump in certificate is dated before the lot date, is that just sloppiness 14:32
  • tail_factor — does purity by hplc at one wavelength miss things 15:26
AN

a lab that reports "greater than 98%" rather than a number is telling you they did not integrate carefully, thats just me

peak   RRT    area%    note
  1   0.42     0.31    solvent front
  2   0.88     0.44    related substance
  3   1.00    98.72    main
  4   1.14     0.53    related substance
NN

tfa or acetate, how do i tell from the paperwork

i have never seen a research certificate with an endotoxin result on it. not once, ill dig out the number

purity is not assay

peak   RRT    area%    note
  1   0.42     0.31    solvent front
  2   0.88     0.44    related substance
  3   1.00    98.72    main
  4   1.14     0.53    related substance
🎉4👀1🧊1

for the archive purity is what fraction of the contents is the target. assay is how many mg are actually there. different questions
the certificate from KP is the one i use to teach this because it actually has a populated impurity table

OO

the related substances table is the interesting part. a row of "not detected" means they did not look hard, ill dig out the number

4🧪4📉2
OO

the honest summary is that a certificate tells you what the supplier says about a lot they chose to test, n of 1 obviously

weigh the vial

unrelated but the font on this one changes halfway down, am i being paranoid

HH

retention time shifts between runs are normal. relative retention time is the number to compare

does anyone keep a folder of certificates to compare over time

test it yourself

good certificate actually

🎉1

is sterility tested as part of a normal purity certificate

mixed fonts and inconsistent kerning in one document is worth a second look

two certificates from the same supplier have an identical chromatogram, is that normal

EE

water content is why an honest 10mg vial assays at 9.1. karl fischer titration, and most certificates omit it

why would a vial be 98.6 pure and still assay under label

net peptide is gross mass minus water minus counterion. that is why 11.4mg of powder can be a correct 10mg vial

GV

quick one a supplier certificate on its own is a starting point, not evidence. that is the whole reason the verification channel exists, your mileage will differ

EE

residual solvents matter more than people think for anything that went through a lot of purification steps

GV

gross mass on a jewellery scale plus the water content is enough to catch most underfills

is endotoxin ever tested on research material

same chromatogram

🙏11
QH

coming back to this should a certificate say which instrument and method they used

NN

an identical chromatogram on two different lots is the single biggest tell there is

thats the counterion

OO

a vial can be 99.4% pure and hold 8.1mg of a 10mg label. both numbers are true and only one of them is the one you care about

QH

slightly off topic but one decimal versus two is usually just house style, not precision

NN

for the archive is area percent the same thing as how many mg are in the vial

is there a standard layout or does every lab do their own

TT

sorry to jump in certificate is dated before the lot date, is that just sloppiness

1👍13
NN

quick one i was wrong about this for a year: area percent under-reports nothing, it just answers a different question than assay does, happy to be corrected

thats a real table

14:53tenpence pinned a message
NN

follow up i asked GGPeps for the method and they sent it. that alone put them ahead of most

not evidence on its own

TT

the certificate from SWB is the one i use to teach this because it actually has a populated impurity table

[edited]
RR

a certificate should name the method, the instrument, the column and the operator. most name none of those

6
TF

does purity by hplc at one wavelength miss things

LineClaimsDoes not claim
Purity (area %)fraction of detected material that is the targethow many mg are in the vial
Assay / contentmg of target per vialthat it is sterile
Water contentmass fraction that is wateranything about purity
Counterionsalt form and its mass sharenet peptide unless stated
Related substanceswhat else was seenwhat was not looked for
TT

if you only read one line on a certificate, read the lot number. if you read two, read the assay